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Tissue-Tek® Tissue-Clear®

by Sakura Finetek Europe B.V. 3 variants

Ref 1466Model Tissue-Tek® Tissue-Clear® Xylene Substitute

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number8720177600059122EC Basic UDI-DI 08720177655507UDI-DIDate13 Aug 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Tissue-Tek® Tissue-Clear® Xylene Substitute; 5 L
Model / Reference
Tissue-Tek® Tissue-Clear® Xylene Substitute, 1466
Primary DI / UDI-DI
08720177655507
Basic UDI-DI
8720177600059122EC
EMDN Code
W01030799 Histology / cytology reagents - other
Device Class
Class A
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000023138

Other devices from Sakura Finetek Europe B.V.

See all devices from Sakura Finetek Europe B.V. →

Properties

  • Reagent
  • Professional Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No